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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 604779Generated: October 25, 2026

Hydrochloric Acid → Isoquinolyl 4-methoxyphenyl ketone

https://huagongshe.com/reaction/604779

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant4-BromoanisoleHCID 7730—
Reactant1,2-DibromoethaneHCID 7839—
ReactantSodium HydroxideHCID 14798—
Reactant1-IsoquinolinecarbonitrileHCID 306057—
ReactantMagnesiumHCID 5462224—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
ProductIsoquinolyl 4-methoxyphenyl ketoneHCID 693112—

Reaction Conditions

Temperature0 °C

Reaction Steps

4-Bromoanisol (15.3 ml, 122 mmol) and a catalytic amount of 1,2-dibromoethane as an initiator were added to a mixed solution of magnesium (3059 mg, 125.8 mmol) and tetrahydrofuran (20 ml) under nitrogen atmosphere, and this reaction mixture was stirred while heating under reflux for 45 minutes. The mixture was cooled to 0° C., a solution of 1-isoquinolinecarbonitrile (10.78 g, 69.9 mmol) in tetrahydrofuran (30 ml) was added dropwise thereto, and this reaction mixture was stirred at room temperature for 2 hours. The reaction mixture was cooled on ice, concentrated hydrochloric acid (24 ml) and methanol (120 ml) were added, and this mixture was heated under reflux for 1.5 hours. After cooling on ice, the mixture was adjusted to pH 8 by adding aqueous sodium hydroxide, extracted with ether, washed with saturated brine, dried over anhydrous magnesium sulfate, and then concentrated under reduced pressure. The residue was purified by silica gel column chromatography to give the title compound (15.87 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07910712B2
Source datasetuspto-grants-2011_03
ORD IDord-9a130f8005c04dfaa58a55f87d6fd8f3
Source noteuspto-grants-2011_03